| Identification | More | [Name]
4-Pentyn-1-ol | [CAS]
5390-04-5 | [Synonyms]
4-PENTYN-1-OL
4-PENTYNE-1-OL
1-Pentyn-5-ol
4-Pentyn-1-ol, 98+%
4-Pentin-1-ol 97%
1-Pentyne-5-ol
4-Pentynyl alcohol | [EINECS(EC#)]
226-383-6 | [Molecular Formula]
C5H8O | [MDL Number]
MFCD00002974 | [Molecular Weight]
84.12 | [MOL File]
5390-04-5.mol |
| Chemical Properties | Back Directory | [Appearance]
Clear yellow liquid | [Melting point ]
-24.1°C (estimate) | [Boiling point ]
154-155 °C (lit.) | [density ]
0.904 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.445(lit.)
| [Fp ]
143 °F
| [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [solubility ]
Chloroform, Methanol | [form ]
Liquid | [pka]
14.81±0.10(Predicted) | [color ]
Clear yellow | [Specific Gravity]
0.904 | [Water Solubility ]
Miscible with water. | [BRN ]
1736712 | [InChIKey]
CRWVOXFUXPYTRK-UHFFFAOYSA-N | [CAS DataBase Reference]
5390-04-5(CAS DataBase Reference) | [NIST Chemistry Reference]
4-Pentyn-1-ol(5390-04-5) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
1987 | [WGK Germany ]
3
| [F ]
10 | [HazardClass ]
3.2 | [PackingGroup ]
III | [HS Code ]
29052900 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear yellow liquid | [Uses]
4-Pentyn-1-ol is an alkyne alcohol that is used as an initiator in ring-opening polymerization reactions. 4-Pentyn-1-ol is capable of undergoing cyclosisomerization, and is also used as a reactant in the synthesis of (+)-Serinolamide A, a cannabinoid CB1 receptor agonist. | [Application]
4-Pentyn-1-ol was used in preparation of 3-pent-4-ynyloxy phthalonitrile. It was also used as starting reagent in stereoselective total synthesis of antimicrobial marine metabolites, ieodomycin A and B. | [General Description]
Mechanism of (THF)W(CO)5-promoted endo- and exo-cycloisomerization of 4-pentyn-1-ol was studied. | [Synthesis]
4-Pentyn-1-ol has been prepared from 4-penten-1-ol by bromination followed by dehydrobromination with alkali. |
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